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43 - MDC - Medical Sciences and Clinical Research


MDC 113 - Good Pharmacovigilance Practice

Code Start Date Duration Venue Fees
MDC 113 27 December 2020 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 24 January 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 21 February 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 21 March 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 18 April 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 16 May 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 13 June 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 11 July 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 08 August 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 05 September 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 03 October 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 28 November 2021 5 Days Istanbul $ 3450 Registration Form Link
MDC 113 26 December 2021 5 Days Istanbul $ 3450 Registration Form Link
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Course Description

The pharmaceutical industry is challenged with providing oversight of a drug’s safety throughout the product lifecycle. This includes continually reviewing safety profiles and managing and assessing benefits  and risks that arise during and after drug development.

This course provides detailed coverage of the key pharmacovigilance concepts, global pharmacovigilance systems and regulations according to Good Pharmacovigilance Practice guidelines that support the development of optimal pharmacovigilance programmes.

Course Objectives

  • Introducing ADRs and PV
  • Reporting spontaneous adverse reaction  
  • Learning requirements and recommendations to set up PV system
  • Mastering effective communication in pharmacovigilance
  • Examining pharmacovigilance in Public Health Programmes , vaccines, herbals and PV methods

Who Should Attend?

  • Drug Safety / Pharmacovigilance Staff
  • Regulatory Affairs Staff
  • Clinical Development Staff
  • Clinical Research Organisation Staff

Course Details/Schedule

Day 1

  • The Concept of Pharmacovigilance and Methodology
  • Background and International Context
  • General Information on Reporting System
  • GPP General Principles
  • Setting up National Pharmacovigilance Systems and Centers
  • Basic Activities for Setting up a Pharmacovigilance Center

Day 2

  • PV Documentation, Characteristics of Reports and Other Documents
  • Computer Systems
  • Management of Reports (Submitting Reports, Data Coding and Entry, Characteristics of Reporting
  • Review of the Database, Assessing Reports)
  • Pharmacovigilance in Clinical Studies
     

Day 3

  • Identification of Risks
  • Descriptive Analysis of a Series of Cases
  • Use of Data Mining to Identify Associations between Medicines and Adverse Events
  • Generation of Signals
  • Quantification of Risks
  • Quantification of the Strength of Association
  • Studies to Quantify Risks

Day 4

  • Risk Assessment, Assessment of the Benefit/Risk Ratio
  • Risk Management and Communication
  • Periodic Safety Update Reports
  • Publication and Information in Pharmacovigilance
  • Crisis Management
  • Risk Prevention

Day 5

  • Evaluation of the Pharmacovigilance System
  • National Regulatory Authority
  • Essential Elements of Effective Pharmacovigilance
  • Relations with Marketing Authorization Holders
  • Certification of GPP in the Pharmaceutical Industry
  • National Pharmacovigilance System
  • National and Local Pharmacovigilance Centers
  • Public Health and Immunization Programs